Singla Nirmish, Krabbe Laura-Maria, Aydin Ahmet M, Panwar Vandana, Woldu Solomon L, Freifeld Yuval, Wood Christopher G, Karam Jose A, Weizer Alon Z, Raman Jay D, Remzi Mesut, Rioux-Leclercq Nathalie, Haitel Andrea, Roscigno Marco, Bolenz Christian, Bensalah Karim, Sagalowsky Arthur I, Shariat Shahrokh F, Lotan Yair, Bagrodia Aditya, Kapur Payal, Margulis Vitaly
Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.
Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX; Department of Urology, University of Muenster Medical Center, Muenster, Germany.
Urol Oncol. 2018 Jul;36(7):343.e1-343.e8. doi: 10.1016/j.urolonc.2018.04.004. Epub 2018 May 7.
Enhancer of zeste homolog 2 is a methyltransferase encoded by the EZH2 gene, whose role in upper tract urothelial carcinoma (UTUC) is poorly understood. We sought to evaluate the prognostic value of EZH2 expression in UTUC.
We reviewed a multi-institutional cohort of patients who underwent radical nephroureterectomy for high-grade UTUC from 1990 to 2008. Immunohistochemistry for EZH2 was performed on tissue microarrays. Percentage of staining was evaluated, and the discriminative value of EZH2 was tested, with EZH2 positivity defined as>20% staining present. Clinicopathologic characteristics and oncologic outcomes (recurrence-free (RFS), cancer-specific (CSS), and overall survival (OS)) were compared, stratified by EZH2 positivity. The prognostic role of EZH2 was assessed using Kaplan-Meier, univariate (UVA), and multivariate (MVA) Cox regression analyses. Significance was defined for P<0.05.
A total of 376 patients were included for analysis, with median follow-up 36.0 months. Overall, 78 (20.7%) were EZH2-positive. EZH2 expression was more often associated with ureteral location, lymphovascular invasion, sessile architecture, necrosis, and concomitant carcinoma in situ. On UVA, increased EZH2 expression was a significant predictor for inferior RFS (HR 1.63, P = 0.033), CSS (HR 2.03, P = 0.003), and OS (HR 2.11, P<0.001). On MVA EZH2 remained a significant predictor of worse CSS (HR 1.99 [95% CI: 1.21-3.27], P = 0.007) and OS (HR 1.54 [95% CI: 1.06-2.24], P = 0.024), while significance was lost for RFS.
Increased EZH2 expression is associated with adverse pathologic features and inferior oncologic outcomes in patients with high-grade UTUC. The role of EZH2 biology in UTUC pathogenesis remains to be further elucidated.
zeste 同源物 2 增强子是一种由 EZH2 基因编码的甲基转移酶,其在上尿路尿路上皮癌(UTUC)中的作用尚不清楚。我们试图评估 EZH2 表达在 UTUC 中的预后价值。
我们回顾了 1990 年至 2008 年因高级别 UTUC 接受根治性肾输尿管切除术的多机构队列患者。在组织微阵列上进行 EZH2 的免疫组织化学检测。评估染色百分比,并测试 EZH2 的判别价值,EZH2 阳性定义为染色>20%。比较临床病理特征和肿瘤学结局(无复发生存期(RFS)、癌症特异性生存期(CSS)和总生存期(OS)),按 EZH2 阳性分层。使用 Kaplan-Meier、单因素(UVA)和多因素(MVA)Cox 回归分析评估 EZH2 的预后作用。P<0.05 定义为具有统计学意义。
共纳入 376 例患者进行分析,中位随访时间为 36.0 个月。总体而言,78 例(20.7%)为 EZH2 阳性。EZH2 表达更常与输尿管部位、淋巴管浸润、无蒂结构、坏死和原位癌并存相关。在单因素分析中,EZH2 表达增加是 RFS 较差(风险比[HR]1.63,P = 0.033)、CSS(HR 2.03,P = 0.003)和 OS(HR 2.11,P<0.001)明显的预测因素。在多因素分析中,EZH2 仍然是 CSS 较差(HR 1.99[95%置信区间:1.21 - 3.27],P = 0.007)和 OS(HR 1.54[95%置信区间:1.06 - 2.24],P = 0.024)的显著预测因素,而 RFS 则失去统计学意义。
EZH2 表达增加与高级别 UTUC 患者的不良病理特征和较差的肿瘤学结局相关。EZH2 生物学在 UTUC 发病机制中的作用仍有待进一步阐明。